13 research outputs found

    Charge states of low energy ions from the sun

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    Measurements of ionization states and energy spectra of carbon, oxygen, and iron accelerated in ten solar flare particle events are reported, for energies between 15 keV per nucleon and 600 keV per nucleon. The ionization states were remarkably constant from flare to flare, despite great variations in other event parameters. The mean ionization state for carbon was 5.7, for oxygen 6.2, and for iron 11.7, values which are similar to the respective ionization states in the solar wind. The time profile of the He/C+N+O ratio was examined, and it was found that the ratio was small early in the event, and increased with time. The energy spectra of the medium ions showed a flattening below 100 keV per nucleon, which was highly correlated with event size as measured by the event averaged flux of 130 to 220 keV protons

    A direct measurement of the charge states of energetic iron emitted by the sun

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    The charge states of energetic iron have been measured directly for the first time in a solar particle event. In the energy interval 0.01 to 0.25 MeV per nucleon, iron is not fully stripped but has a mean ionization state of 11.6. This value is remarkably similar to the mean ionization state of iron in the quiet solar wind and suggests that the charge states were "frozen-in" at a coronal temperature of approximately 1,500,000 K

    Emission of nearly stripped carbon and oxygen from the sun

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    Energy spectra of nearly stripped carbon and oxygen nuclei were observed during several solar particle events indicating a systematic deviation of these spectra from a simple power law. The spectra bend below 100 keV per nucleon and the degree of turn-over are highly correlated with the size of the flare, as measured by the event averaged flux of 130 to 220 keV protons. The energy spectra of helium computed for the same time periods do not show a similar feature. A large variability of the alpha/CNO ratio from event to event (from 2 to about 20 at 40 keV per nucleon) is found, and, in all cases examined, the carbon and oxygen nuclei are nearly fully stripped. These results are interpreted as evidence for storage of energetic ions in hot (T sub e is approximatey 1.5 million K) coronal regions, followed by strong adiabatic deceleration

    Vertical Field-Effect Transistor Based on Wavefunction Extension

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    We demonstrate a mechanism for a dual layer, vertical field-effect transistor, in which nearly-depleting one layer will extend its wavefunction to overlap the other layer and increase tunnel current. We characterize this effect in a specially designed GaAs/AlGaAs device, observing a tunnel current increase of two orders of magnitude at cryogenic temperatures, and we suggest extrapolations of the design to other material systems such as graphene

    Anastral spindle assembly and γ-tubulin in Drosophila oocytes

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    <p>Abstract</p> <p>Background</p> <p>Anastral spindles assemble by a mechanism that involves microtubule nucleation and growth from chromatin. It is still uncertain whether γ-tubulin, a microtubule nucleator essential for mitotic spindle assembly and maintenance, plays a role. Not only is the requirement for γ-tubulin to form anastral <it>Drosophila </it>oocyte meiosis I spindles controversial, but its presence in oocyte meiosis I spindles has not been demonstrated and is uncertain.</p> <p>Results</p> <p>We show, for the first time, using a bright GFP fusion protein and live imaging, that the <it>Drosophila </it>maternally-expressed γTub37C is present at low levels in oocyte meiosis I spindles. Despite this, we find that formation of bipolar meiosis I spindles does not require functional γTub37C, extending previous findings by others. Fluorescence photobleaching assays show rapid recovery of γTub37C in the meiosis I spindle, similar to the cytoplasm, indicating weak binding by γTub37C to spindles, and fits of a new, potentially more accurate model for fluorescence recovery yield kinetic parameters consistent with transient, diffusional binding.</p> <p>Conclusions</p> <p>The FRAP results, together with its mutant effects late in meiosis I, indicate that γTub37C may perform a role subsequent to metaphase I, rather than nucleating microtubules for meiosis I spindle formation. Weak binding to the meiosis I spindle could stabilize pre-existing microtubules or position γ-tubulin for function during meiosis II spindle assembly, which follows rapidly upon oocyte activation and completion of the meiosis I division.</p

    A Versatile Microfluidic Device for Automating Synthetic Biology

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    New microbes are being engineered that contain the genetic circuitry, metabolic pathways, and other cellular functions required for a wide range of applications such as producing biofuels, biobased chemicals, and pharmaceuticals. Although currently available tools are useful in improving the synthetic biology process, further improvements in physical automation would help to lower the barrier of entry into this field. We present an innovative microfluidic platform for assembling DNA fragments with 10× lower volumes (compared to that of current microfluidic platforms) and with integrated region-specific temperature control and on-chip transformation. Integration of these steps minimizes the loss of reagents and products compared to that with conventional methods, which require multiple pipetting steps. For assembling DNA fragments, we implemented three commonly used DNA assembly protocols on our microfluidic device: Golden Gate assembly, Gibson assembly, and yeast assembly (i.e., TAR cloning, DNA Assembler). We demonstrate the utility of these methods by assembling two combinatorial libraries of 16 plasmids each. Each DNA plasmid is transformed into Escherichia coli or Saccharomyces cerevisiae using on-chip electroporation and further sequenced to verify the assembly. We anticipate that this platform will enable new research that can integrate this automated microfluidic platform to generate large combinatorial libraries of plasmids and will help to expedite the overall synthetic biology process
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